Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G Michael Vincent

Showing results (1-10 of 38) with videos related to

Pageof 4
Sort By:
Indian Pacing and Electrophysiology Journal|September 5, 2006
The long QT syndromeG Michael Vincent
Seminars in Pediatric Neurology|June 3, 2005
The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death in children and young adultsG Michael Vincent
Pacing and Clinical Electrophysiology : PACE|July 16, 2009
Sudden cardiac arrest in the young due to inherited arrhythmias: the importance of family careG Michael Vincent
The New England Journal of Medicine|May 9, 2003
The long-QT syndrome--bedside to bench to bedsideG Michael Vincent
Journal of Cardiovascular Electrophysiology|October 3, 2003
Atrial arrhythmias in the inherited long QT syndrome: laboratory quirk or clinical arrhythmia?G Michael Vincent
Heart Rhythm|April 21, 2005
Risk assessment in long QT syndrome: the Achilles heel of appropriate treatmentG Michael Vincent
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Genotyping has a minor role in selecting therapy for congenital long-QT syndromes at presentG Michael Vincent
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 8, 2005
The role of genotyping in diagnosing cardiac channelopathies : progress to dateG Michael Vincent, Li Zhang
Cardiac Electrophysiology Review|May 2, 2002
Congenital Long QT syndromeG Michael Vincent, Katherine Timothy, Li Zhang
Circulation|June 20, 2007
Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndromeQiuming Gong, Li Zhang, G Michael Vincent, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Indian Pacing and Electrophysiology Journal|September 5, 2006
The long QT syndromeG Michael Vincent
Seminars in Pediatric Neurology|June 3, 2005
The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death in children and young adultsG Michael Vincent
Pacing and Clinical Electrophysiology : PACE|July 16, 2009
Sudden cardiac arrest in the young due to inherited arrhythmias: the importance of family careG Michael Vincent
The New England Journal of Medicine|May 9, 2003
The long-QT syndrome--bedside to bench to bedsideG Michael Vincent
Journal of Cardiovascular Electrophysiology|October 3, 2003
Atrial arrhythmias in the inherited long QT syndrome: laboratory quirk or clinical arrhythmia?G Michael Vincent
Heart Rhythm|April 21, 2005
Risk assessment in long QT syndrome: the Achilles heel of appropriate treatmentG Michael Vincent
Circulation. Arrhythmia and Electrophysiology|October 8, 2009
Genotyping has a minor role in selecting therapy for congenital long-QT syndromes at presentG Michael Vincent
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|November 8, 2005
The role of genotyping in diagnosing cardiac channelopathies : progress to dateG Michael Vincent, Li Zhang
Cardiac Electrophysiology Review|May 2, 2002
Congenital Long QT syndromeG Michael Vincent, Katherine Timothy, Li Zhang
Circulation|June 20, 2007
Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndromeQiuming Gong, Li Zhang, G Michael Vincent, et al.
Pageof 4